Literature DB >> 12705495

Pathological structure of the kidney from adult mice with mosaic mutation.

M Lenartowicz1, M Kowal, D Buda-Lewandowska, J Styrna.   

Abstract

The mosaic (Atp7a(mo-ms)) is an X-linked, lethal mutation in mice. In mosaic mutant males, many clinical features characteristic of defective copper metabolism have been observed and they die at the age of 15 days, exhibiting strong similarities to the brindled and macular mutants. About 4% of the mutant males live to sexual maturity and some of them are fertile. In this paper, alterations in the structure of the kidney from adult mutants are described. Owing to an inherited defect of efflux, copper is accumulated in the kidney of the mutants up to a toxic level and this leads to severe damage of the renal cortex. Pathological changes in the kidney mostly affected the structure of the renal corpuscle and renal tubules.

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Year:  2002        PMID: 12705495     DOI: 10.1023/a:1022877130344

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  24 in total

1.  Urologic abnormalities in Menkes' kinky hair disease: report of three cases.

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Journal:  J Pediatr Surg       Date:  1997-05       Impact factor: 2.545

Review 2.  A delicate balance: homeostatic control of copper uptake and distribution.

Authors:  M M Peña; J Lee; D J Thiele
Journal:  J Nutr       Date:  1999-07       Impact factor: 4.798

3.  Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease.

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Journal:  Pediatr Res       Date:  1997-10       Impact factor: 3.756

4.  A comparison of phenotype and copper distribution in blotchy and brindled mutant mice and in nutritionally copper deficient controls.

Authors:  M Phillips; J Camakaris; D M Danks
Journal:  Biol Trace Elem Res       Date:  1991-04       Impact factor: 3.738

5.  Analysis of the distribution of Cu, Fe and Zn and other elements in brindled mouse kidney using a scanning proton microprobe.

Authors:  B J Kirby; D M Danks; G J Legge; J F Mercer
Journal:  J Inorg Biochem       Date:  1998-09       Impact factor: 4.155

6.  Copper-metallothionein from the toxic milk mutant mouse enhances lipid peroxidation initiated by an organic hydroperoxide.

Authors:  G F Stephenson; H M Chan; M G Cherian
Journal:  Toxicol Appl Pharmacol       Date:  1994-03       Impact factor: 4.219

7.  Changes in tissue growth, concentrations of copper, iron, cytochrome oxidase and superoxide dismutase subsequent to dietary or genetic copper deficiency in mice.

Authors:  J R Prohaska
Journal:  J Nutr       Date:  1983-10       Impact factor: 4.798

Review 8.  Lead nephrotoxicity and associated disorders: biochemical mechanisms.

Authors:  C V Nolan; Z A Shaikh
Journal:  Toxicology       Date:  1992       Impact factor: 4.221

Review 9.  Newer aspects of micronutrients in chronic disease: copper.

Authors:  J J Strain
Journal:  Proc Nutr Soc       Date:  1994-11       Impact factor: 6.297

10.  Histochemical localization of copper in the intestine and kidney of macular mice: light and electron microscopic study.

Authors:  H Kodama; T Abe; M Takama; I Takahashi; M Kodama; M Nishimura
Journal:  J Histochem Cytochem       Date:  1993-10       Impact factor: 2.479

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  3 in total

Review 1.  Molecular Regulation of Copper Homeostasis in the Male Gonad during the Process of Spermatogenesis.

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Journal:  Int J Mol Sci       Date:  2020-11-28       Impact factor: 5.923

2.  Decreased Expression of the Slc31a1 Gene and Cytoplasmic Relocalization of Membrane CTR1 Protein in Renal Epithelial Cells: A Potent Protective Mechanism against Copper Nephrotoxicity in a Mouse Model of Menkes Disease.

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Journal:  Int J Mol Sci       Date:  2022-09-28       Impact factor: 6.208

Review 3.  Mottled Mice and Non-Mammalian Models of Menkes Disease.

Authors:  Małgorzata Lenartowicz; Wojciech Krzeptowski; Paweł Lipiński; Paweł Grzmil; Rafał Starzyński; Olga Pierzchała; Lisbeth Birk Møller
Journal:  Front Mol Neurosci       Date:  2015-12-18       Impact factor: 5.639

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